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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
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Institution Date Title Author
國立臺灣師範大學 2019-09-05T05:45:45Z 台灣銀葉粉蝨懷菌細胞於超微形態上及基因體之研究 吳佩臻; Pei-Chen Wu
國立臺灣師範大學 2019-08-28T07:19:12Z 桃園縣學校志工領導人正向領導策略與工作滿意之關係研究 吳霈宸; Pei-Chen Wu
亞洲大學 2014-03 Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET Chih-Ping Chen;Yi-Ning Su;Shee-Uan Chen;Tung-Yao Chang;Pei-Chen Wu;Schu-Rern Chern;Peih-Shan Wu;Yu-Ling Kuo;Wayseen Wang
中國醫藥大學 2014-03 Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET 陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Shee-Uan Chen);(Tung-Yao Chang);(Pei-Chen Wu);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ling Kuo);(Wayseen Wang)
中國醫藥大學 2013-12 Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review 陳持平(Chih-Ping Chen)*;(Tung-Yao Chang);(Wan-Yuo Guo);(Pei-Chen Wu);(Liang-Kai Wang);(Schu-Rern Chern);(Peih-Shan Wu);蘇俊維(Jun-Wei Su);(Yu-Ting Chen);(Li-Feng Chen);(Wayseen Wang)
元智大學 2013 社會臨場感、表達性導向及利益性導向對臉書按讚行為影響之探討 吳沛晨; Pei-Chen Wu
中國醫藥大學 2012-12 Detection of mosaic balanced homologous acrocentric rearrangement rea(21q21q) in a woman with repeated pregnancy losses 陳持平(Chih-Ping Chen)*;(Pei-Chen Wu);蔡輔仁(Fuu-Jen Tsai);(Li-Feng Chen);(Wayseen Wang)
輔英科技大學 2012-10-01 Cell cycle regulation by bevacizumab in ARPE-19 human retinal pigment epithelial cells Chien-Neng Kuo;Chung-Yi Chen;Chien-Hsiung Lai;Li-Ju Lai;Pei-Chen Wu;Chia-Hui Hung;Ching-Hsein Chen
中國醫藥大學 2012-09 Monozygotic twins with trisomy 18 of paternal origin: prenatal diagnosis and molecular cytogenetic characterization in a pregnancy with one structurally abnormal living fetus and one intrauterine fetal demise 陳持平(Chih-Ping Chen)*;(Schu-Rern Chern);(Yi-Yung Chen);(Pei-Chen Wu);(Dai-Dyi Town);(Wen-Lin Chen);(Wayseen Wang)
中國醫藥大學 2012-09 Rapid aneuploidy diagnosis of trisomy 18 by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal arachnoid cyst detected in late second trimester 陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Shun-Long Weng);(Fuu-Jen Tsai);(Chen-Yu Chen);(Yu-Peng Liu);(Schu-Rern Chern);(Wen-Lin Chen);(Pei-Chen Wu);(Wayseen Wang)
中國醫藥大學 2012-04 Persistent cloaca presenting with a perineal cyst: prenatal ultrasound and magnetic resonance imaging findings 陳持平(Chih-Ping Chen)*;(Tung-Yao Chang);(Chin-Yuan Hsu);(Yu-Peng Liu);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Wayseen Wang)
中國醫藥大學 2012-03 Short rib-polydactyly syndrome type II (Majewski): prenatal diagnosis, perinatal imaging findings and molecular genetic analysis 陳持平(Chih-Ping Chen)*;(Tung-Yao Chang);(Tao-Yeuan Wang);(Chen-Yu Chen);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Schu-Rern Chern);(Wayseen Wang)
中國醫藥大學 2012-03 Rapid aneuploidy diagnosis of partial trisomy 7q (7q34->qter) and partial monosomy 10q (10q26.12->qter) by array comparative genomic hybridization using uncultured amniocytes 陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Yi-Ning Su);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Dai-Dyi Town);(Li-Feng Chen);(Meng-Shan Lee);(Wayseen Wang)
元智大學 2012 我國航空業節能減碳之探討-以長榮航空為例 吳珮甄; Pei-Chen Wu
中國醫藥大學 2011-12 A de novo duplication of chromosome 21q22.11->qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings 陳持平(Chih-Ping Chen)*;(Hsu-Kuaing Huang);(Pei-Ying Lin);(Yi-Ning Su);(Ming Chen);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Schu-Rern Chern);(Yu-Ting Chen);(Chen-Chi Lee);(Wayseen Wang)
中國醫藥大學 2011-09 A 24.2-Mb deletion of 4q12->q21.21 characterized by array CGH in a 13?-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed puberty 陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Yi-Ning Su);(Schu-Rern Chern);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Li-Feng Chen);(Wayseen Wang)
中國醫藥大學 2011-09 De novo duplication Xq22.1->q24 with a disruption of the NXF geen cluster in a mentally retarded woman with short stature and premature ovarian failure 陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Hung-Hung Lin);(Schu-Rern Chern);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Chen-Chi Lee);(Yu-Ting Chen);(Wayseen Wang)
中國醫藥大學 2011-09 Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia 陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Yi-Yung Chen);(Schu-Rern Chern);(Yu-Peng Liu);(Pei-Chen Wu);(Chen-Chi Lee);(Yu-Ting Chen);(Wayseen Wang)
中國醫藥大學 2011-09 Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation 陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Ming Chen);(Jain-Pei Huang);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Wen-Lin Chen);(Wayseen Wang)
中國醫藥大學 2011-09 Mosaic ring chromosome 4 in a child with mild dysmorphisms, congenital heart defects and developmental delay 陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Yi-Ning Su);(Schu-Rern Chern);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Chen-Chi Lee);(Wayseen Wang)
中國醫藥大學 2011-09 Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization and perinatal findings in a fetus with dup(15)(q26.2q26.3) 陳持平(Chih-Ping Chen)*;(Yi-Hui Lin);(Heng-Kien Au);(Chin-Yuan Hsu);(Yu-Peng Liu);(Pei-Chen Wu);(Schu-Rern Chern);(Yu-Ting Chen);(Li-Feng Chen);(Adam Hwa-Ming Hsieh);(Wayseen Wang)
中國醫藥大學 2011-09 Prenatal diagnosis of microvillus inclusion disease 陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Schu-Rern Chern);(Pei-Chen Wu);(Wayseen Wang)
亞洲大學 2011-06 Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p 陳持平;Chen, Chih-Ping;Yi-Ning Su;Schu-Rern Chern;Fuu-Jen Tsai;Pei-Chen Wu;Chen-Chi Lee;Wayseen Wang
中國醫藥大學 2011-06 Rapid aneuploidy diagnosis by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal nuchal edema and mild ascites 陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Pei-Chen Wu);(Chen-Chi Lee);(Chen-Wen Pan);(Wayseen Wang)
中國醫藥大學 2011-06 Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis 陳持平(Chih-Ping Chen)*;(Jui-Der Liou);(Chi-Hsin Chiang);(Yi-Ning Su);(Schu-Rern Chern);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Yu-Ting Chen);(Chen-Chi Lee);(Wen-Lin Chen);(Wayseen Wang)
中國醫藥大學 2011-06 Prenatal diagnosis of cerebral tubers by magnetic resonance imaging following detection of cardiac rhabdomyomas by prenatal ultrasound in a fetus with a nonsense mutation in the TSC2 gene 陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Chin-Yuan Hsu);(Ming-Ren Chen);(Yu-Peng Liu);(Pei-Chen Wu);(Wayseen Wang)
中國醫藥大學 2011-03 Unbalanced reciprocal translocations at amniocentesis 陳持平(Chih-Ping Chen)*; (Pei-Chen Wu); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Dai-Dyi Town); (Wen-Lin Chen); (Li-Feng Chen); (Meng-Shan Lee); (Chen-Wen Pan); (Wayseen Wang)
中國醫藥大學 2011-03 Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization 陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); (Chin-Yuan Hsu); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Yu-Ting Chen); (Meng-Shan Lee); (Wayseen Wang)
中國醫藥大學 2011-03 Pathological characterization of a malformed umbilical cord associated with body stalk anomaly 陳持平(Chih-Ping Chen)*; (Tao-Yeuan Wang); (Pei-Chen Wu); 蔡輔仁(Fuu-Jen Tsai); (Wayseen Wang)
中國醫藥大學 2011-03 Congenital tracheal stenosis in a boy with the 22q13.3 deletion syndrome 陳持平(Chih-Ping Chen)*; (Shuan-Pei Lin); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Pei-Chen Wu); (Chen-Chi Lee); (Meng-Shan Lee); (Yu-Ting Chen); (Wayseen Wang)
中國醫藥大學 2011-03 Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations 陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Shin-Yu Lin); (Chih-Long Chang); (Yeou-Lih Wang); (Jiau-Pei Huang); (Chen-Yu Chen); (Fang-Yu Hung); (Yi-Yung Chen); (Pei-Chen Wu); (Wayseen Wang)
亞洲大學 2010-12 Ellis-van Creveld syndrome: prenatal diagnosis, molecular analysis and genetic counseling Chih-Ping Chen; Yi-Ning Su;Chin-Yuan Hsu;Schu-Rern Chern;Fuu-Jen Tsai;Pei-Chen Wu;Po-Tsang Chen;Wayseen Wang
中國醫藥大學 2010-12 Prenatal diagnosis of partial monosomy 1q (1q42.3->qter) associated with hydrocephalus and corpus callosum agenesis 陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Pei-Chen Wu); (Chen-Chi Lee); (Chen-Wen Pan); (Wayseen Wang)
中國醫藥大學 2010-12 A 5.3-Mb duplication of 9p12->p13.1 characterized by array CGH in a female infant with developmental delay 陳持平(Chih-Ping Chen)*; (Shuan-Pei Lin); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chen-Chi Lee); (Chen-Wen Pan); (Pei-Chen Wu); (Wayseen Wang)
中國醫藥大學 2010-12 Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings 陳持平(Chih-Ping Chen)*; (Ming Chen); (Yi-Ning Su); (Chin-Yuan Hsu); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Pei-Chen Wu); (Chen-Chi Lee); (Wayseen Wang)
中國醫藥大學 2010-12 Balanced reciprocal translocations at amniocentesis 陳持平(Chih-Ping Chen)*; (Pei-Chen Wu); (Yi-Ning Su); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chen-Chi Lee); (Dai-Dyi Town); (Wen-Lin Chen); (Li-Feng Chen); (Meng-Shan Lee); (Chen-Wen Pan); (Wayseen Wang)
中國醫藥大學 2010-12 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8 陳持平(Chih-Ping Chen)*; (Ming Chen); (Tsang-Ming Ko); (Gwo-Chin Ma); 蔡輔仁(Fuu-Jen Tsai); (Ming-Song Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Li-Feng Che); (Wayseen Wang)
中國醫藥大學 2010-12 Partial trisomy 16p (16p12.2->pter) and partial monosomy 22q (22q13.31->qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization 陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Richard Shih-Hung Young); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Schu-Rern Chern); (Dai-Dyi Town); (Chen-Wen Pan); (Wayseen Wang)
中國醫藥大學 2010-12 Partial trisomy 10q (10q25.1->qter) and partial monosomy 13q (13q34->qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization 陳持平(Chih-Ping Chen)*; (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Schu-Rern Chern); (Pei-Chen Wu); (Chen-Chi Lee); (Wen-Lin Chen); (Wayseen Wang)
中國醫藥大學 2010-12 Recurrent distal 16q duplication and terminal 22q deletion: prenatal diagnosis and genetic counseling 陳持平(Chih-Ping Chen)*; (Ming-Chao Huang); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Dai-Dyi Town); (Chen-Wen Pan); (Wayseen Wang)
中國醫藥大學 2010-12 Ellis-van Creveld syndrome: prenatal diagnosis, molecular analysis and genetic counseling 陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Chin-Yuan Hsu); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Po-Tsang Chen); (Wayseen Wang)
中國醫藥大學 2010-09 Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q 陳持平(Chih-Ping Chen)*; 蔡輔仁(Fuu-Jen Tsai); (Chen-Chi Lee); (Wen-Lin Chen); (Chen-Wen Pan); (Pei-Chen Wu); (Wayseen Wang)
中國醫藥大學 2010-09 A de novo 7.9 Mb deletion in 22q13.2->qter in a boy with autistic features, epilepsy, developmental delay atopic dermatitis and abnormal immunological findings 陳持平(Chih-Ping Chen)*; (Shuan-Pei Li); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Yu-Ting Chen); (Wayseen Wang)
中國醫藥大學 2010-09 Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3->pter) and partial monosomy 13q (13q33.3->qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly 陳持平(Chih-Ping Chen)*; (Ming Chen); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chin-Yuan Hsu); (Pei-Chen Wu); (Dai-Dyi Town); (Dong-Jay Lee); (Gwo-Chin Ma); (Wayseen Wang)
中國醫藥大學 2010-09 Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization 陳持平(Chih-Ping Chen)*; (Yung-Ting Guo); (Shuan-Pei Lin); (Yi-Ning Su); (Yann-Jang Chen); (Rui-Yuan Hseuh); (Yi-Hui Lin); (Pei-Chen Wu); (Chen-Chi Lee); (Yu-Ting Chen); (Wayseen Wang)
中國醫藥大學 2010-09 Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses 陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); (Yu-Ming Hwu); (Shuan-Pei Lin); (Chyong-Hsin Hsu); 蔡輔仁(Fuu-Jen Tsai); (Tao-Yeuan Wang); (Pei-Chen Wu); (Chen-Chi Lee); (Yu-Ting Chen); (Li-Feng Chen); (Wayseen Wang)
中國醫藥大學 2010-09 Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses 陳持平(Chih-Ping Chen)*; (Hsien-Ming Lin); (Yi-Ning Su); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Yu-Ting Chen); (Meng-Shan Lee); (Chen-Wen Pan); (Wayseen Wang)
中國醫藥大學 2010-09 Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy 陳持平(Chih-Ping Chen)*; (Yu-Peng Liu); (Tung-Yao Chang); 蔡輔仁(Fuu-Jen Tsai); (Chen-Yu Chen); (Pei-Chen Wu); (Teresa Hsiao-Tien Chen); (Wayseen Wang)
中國醫藥大學 2010-09 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21 陳持平(Chih-Ping Chen)*; (Chyi-Chyang Lin); (Tsang-Ming Ko); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chen-Chi Lee); (Yu-Ting Chen); (Pei-Chen Wu); (Wayseen Wang)
中國醫藥大學 2010-09 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22 陳持平(Chih-Ping Chen)*; (Chyi-Chyang Lin); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chen-Chi Lee); (Wen-Ling Chen); (Li-Feng Chen); (Pei-Chen Wu); (Wayseen Wang)

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